HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(Isocyanatomethyl)-2-methylbenzene → HCID 22649283, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(Isocyanatomethyl)-2-methylbenzene | HCID 2733386 | — |
| Reactant | 4-amino-6-methoxy-7-(N-methylpiperidin-4-ylmethoxy)quinazoline | HCID 22243908 | — |
| Product | HCID 22649283 | HCID 22649283 | — |
Reaction Steps
Using an analogous procedure to that described in Example 3, 2-methylbenzyl isocyanate was reacted with 4-amino-6-methoxy-7-(N-methylpiperidin-4-ylmethoxy)quinazoline. The resultant solid was purified by column chromatography on silica using increasingly polar mixtures of methylene chloride, methanol and a 1% aqueous ammonium hydroxide solution as eluent. There was thus obtained the title compound; NMR Spectrum: (CDCl3) 1.39-1.56 (m, 2H), 1.84-2.04 (m, 5H), 2.29 (s, 3H), 2.39 (s, 3H), 2.9 (d, 2H), 3.92 (s, 3H), 4.03 (d, 2H), 4.66 (d, 2H), 7.21 (m, 4H), 7.34 (m, 2H), 8.6 (s, 1H), 8.74 (s, 1H), 10.44 (t, 1H); Mass Spectrum: M+H+ 450.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06806274B1 |
| Source dataset | uspto-grants-2004_10 |
| ORD ID | ord-953a85823644415b8b89b264237ecd66 |
| Source note | uspto-grants-2004_10 |